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Pharmazie ; 48(5): 340-2, 1993 May.
Article in German | MEDLINE | ID: mdl-8327561

ABSTRACT

The synthesis of some amidrazones as bioisosteric diazaallyl radicals is described starting from the reaction mechanism of the lipoxygenases which postulates the existence of a radical after hydrogen abstraction from the arachidonic acid, N1,N3-diaryl-, N1-aryl-N3-alkyl-benzamidrazones and N1-arylacetamidrazones are strong inhibitors of the soja lipoxygenase.


Subject(s)
Hydrazones/chemical synthesis , Lipoxygenase Inhibitors/chemical synthesis , Hydrazones/pharmacology , Lipoxygenase Inhibitors/pharmacology , Methionine/metabolism , Oxidation-Reduction , Glycine max/enzymology
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